|
ENST00000395796.8:c.*1025G>T
|
ENSP00000379142.4:n.*1025G>T
|
|
|
ENST00000616242.5:c.*147G>T
|
ENSP00000482149.2:n.*147G>T
|
|
|
ENST00000683378.1:n.253G>T
|
|
|
|
ENST00000336642.9:c.61G>T
|
ENSP00000338009.5:p.Gly21Cys
|
|
|
ENST00000345378.7:c.1030G>T
|
ENSP00000223366.2:p.Gly344Cys
|
|
|
ENST00000403799.8:c.1027G>T
MANE Select
|
ENSP00000384247.3:p.Gly343Cys
|
|
|
ENST00000671824.1:c.1090G>T
|
ENSP00000500264.1:p.Gly364Cys
|
|
|
ENST00000672743.1:n.39G>T
|
|
|
|
ENST00000673284.1:c.1027G>T
|
ENSP00000499852.1:p.Gly343Cys
|
|
|
ENST00000336642.8:c.79G>T
|
ENSP00000338009.4:p.Gly27Cys
|
|
|
ENST00000345378.6:c.1030G>T
|
ENSP00000223366.2:p.Gly344Cys
|
|
|
ENST00000395796.7:c.1024G>T
|
ENSP00000379142.3:p.Gly342Cys
|
|
|
ENST00000403799.7:c.1027G>T
|
ENSP00000384247.3:p.Gly343Cys
|
|
|
ENST00000437084.1:c.976G>T
|
ENSP00000402840.1:p.Gly326Cys
|
|
|
ENST00000459642.1:n.407G>T
|
|
|
|
ENST00000473353.1:n.325G>T
|
|
|
|
ENST00000616242.4:c.1024G>T
|
ENSP00000482149.1:p.Gly342Cys
|
|
|
NM_000162.3:c.1027G>T
|
NP_000153.1:p.Gly343Cys
|
|
|
NM_033507.1:c.1030G>T
|
NP_277042.1:p.Gly344Cys
|
|
|
NM_033508.1:c.1024G>T
|
NP_277043.1:p.Gly342Cys
|
|
|
NM_000162.4:c.1027G>T
|
NP_000153.1:p.Gly343Cys
|
|
|
NM_001354800.1:c.1027G>T
|
NP_001341729.1:p.Gly343Cys
|
|
|
NM_001354801.1:c.16G>T
|
NP_001341730.1:p.Gly6Cys
|
|
|
NM_001354802.1:c.-114G>T
|
NP_001341731.1:n.-114G>T
|
|
|
NM_001354803.1:c.61G>T
|
NP_001341732.1:p.Gly21Cys
|
|
|
NM_033507.2:c.1030G>T
|
NP_277042.1:p.Gly344Cys
|
|
|
NM_033508.2:c.1024G>T
|
NP_277043.1:p.Gly342Cys
|
|
|
XM_024446707.1:c.-114G>T
|
XP_024302475.1:n.-114G>T
|
|
|
NM_000162.5:c.1027G>T
MANE Select
|
NP_000153.1:p.Gly343Cys
|
|
|
NM_033507.3:c.1030G>T
|
NP_277042.1:p.Gly344Cys
|
|
|
NM_033508.3:c.1024G>T
|
NP_277043.1:p.Gly342Cys
|
|
|
NM_001354803.2:c.61G>T
|
NP_001341732.1:p.Gly21Cys
|
|
